NDC 44118-702-01 - Plexion

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 44118-702
Requested NDC: 44118-702-01
Package NDCs from labels: 44118-702-01, 44118-702-60
Manufacturer: Eckson Labs LLC
Effective date: 2022-03-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Plexion - Eckson Labs LLC	Eckson Labs LLC	2022-03-30	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
44118-702-01	EA - Each	44118-702	ec552a14-9ef6-4db7-a05c-a011aa0c24fa	1	2022-05-04
44118-702-60	EA - Each	44118-702	e42a49e5-7a00-47a9-8d44-2d87394277a3	1	2022-05-04

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 37 of 37 · 722 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Homeoplex P	ASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), SCROPHULARIA NODOSA, TABEBUIA IMPETIGINOSA, THYROIDINUM (SUIS), FORMICUM ACIDUM, PHOSPHORUS, SILICEA, SULPHUR, THUJA OCCIDENTALIS, AURUM METALLICUM	Supplement Clinic, LLC.	3c0450c8-956e-4788-9e4d-55d30052ca0b	2017-11-01	Warnings	Exact identifier unii: 70FD1KFU70
Inflammation II	ASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), SARSAPARILLA (SMILAX REGELII), TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, THYROIDINUM (SUIS), AURUM METALLICUM, CARBO ANIMALIS, CAUSTICUM, GELSEMIUM SEMPERVIRENS, NATRUM SULPHURICUM, PHOSPHORUS, SULPHUR, THUJA OCCIDENTALIS	BioActive Nutritional, Inc.	4c36e714-f564-41d3-a6b8-60e633defaff	2016-10-04	Warnings	Exact identifier unii: 70FD1KFU70

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.